Senior Clinical Process Associate at IQVIA

Summary

Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.

Responsibilities

• Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
• Establish and maintain effective project/ site communications
• Create and maintain relevant project documents
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
• Participate in document management (creation, review, maintenance, storage, as applicable)
   

Required Skills And Abilities

• Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
• Strong written and verbal communication skills including good command of English language
• Results and detail-oriented approach to work delivery and output
• Good problem solving skills
• Good planning, time management and prioritization skills
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Proven ability to work on multiple projects balancing competing priorities
• Ability to coach/ mentor junior colleagues
   

Minimum Required Education And Experience

• Bachelor's degree in Life Sciences or related field with 1 - 3 years of relevant experience
• Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education.